LDH info

Canonical Allele Identifier: CA16042196
Gene: AGPAT2 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 372106
ClinVar RCV Id: RCV000412609

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136676960C>T , CM000671.2:g.136676960C>T GRCh38
NC_000009.11:g.139571412C>T , CM000671.1:g.139571412C>T GRCh37
NC_000009.10:g.138691233C>T NCBI36
NG_008090.1:g.15500G>A

Transcript Alleles

HGVS Amino-acid change
NM_001012727.1:c.492+1G>A VV NP_001012745.1:p.=
NM_006412.3:c.492+1G>A VV NP_006403.2:p.=
NM_006412.4:c.492+1G>A VV MANE Preferred NP_006403.2:p.=
NM_001012727.2:c.492+1G>A VV NP_001012745.1:p.=
ENST00000371694.7:c.492+1G>A ENSP00000360759.3:p.=
ENST00000371696.6:c.492+1G>A ENSP00000360761.2:p.=
ENST00000472820.1:n.420+1G>A
ENST00000538402.1:c.492+1G>A ENSP00000438919.1:p.=